This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.
Stoccaggio: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Isotipo: IgG
Clonalità: Polyclonal
Coniugazione: Unconjugated
Applicazione: WB;IHC
Diluizione: WB 1:500-1:2000;IHC 1:50-1:200
Simbolo target: NDUFS3
Ig target: CI 30;CI 30KD;CI-30kD;Complex I 30KD;Complex I 30kDa subunit;COMPLEX I;MITOCHONDRIAL RESPIRATORY CHAIN;30-KD SUBUNIT;Complex I-30kD;mitochondrial;NADH coenzyme Q reductase;NADH dehydrogenase (ubiquinone) Fe S protein 3 30kDa;NADH dehydrogenase [ubiquinone] iron sulfur protein 3 mitochondrial;NADH dehydrogenase [ubiquinone] iron-sulfur protein 3;NADH dehydrogenase ubiquinone 30 kDa subunit;NADH-ubiquinone oxidoreductase 30 kDa subunit;NADH-Ubiquinone Oxidoreductase Fe-S Protein 3;NDUFS3;NDUS3
Area di ricerca:Cancer;Cell Biology;Metabolism;Signal Transduction
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